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首页> 外文期刊>ChemCatChem >Upgrading of Biomass Monosaccharides by Immobilized Glucose Dehydrogenase and Xylose Dehydrogenase
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Upgrading of Biomass Monosaccharides by Immobilized Glucose Dehydrogenase and Xylose Dehydrogenase

机译:固定化葡萄糖脱氢酶和木糖脱氢酶通过固定化生物质单糖

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摘要

Direct upgrading and separation of the monosaccharides from biomass liquors is an overlooked area. In this work we demonstrate enzymatic production of gluconic acid and xylonic acid from glucose and xylose present in pretreated birchwood liquor by glucose dehydrogenase (GDH, EC 1.1.1.47) and xylose dehydrogenase (XDH, EC 1.1.1.175), respectively. The biocatalytic conversions were compared using two different kinds of silica support materials (silica nanoparticles (nanoSiO(2)) and porous silica particles with hexagonal pores (SBA 15 silica) for enzyme immobilization. Upon immobilization, both enzymes showed significant improvement in their thermal stability and robustness at alkaline pH and exhibited over 50 % activity even at pH 10 and 60 degrees C on both immobilization matrices. When compared to free enzymes at 45 degrees C, GDH immobilized on nanoSiO(2) and SBA silica displayed a 4.5 and 7.25 fold increase in half-life, respectively, whilst XDH immobilized on nanoSiO(2) and SBA showed a 4.7 and 9.5 fold improvement in half-life, respectively. Additionally, after five reaction cycles both nanoSiO(2)GDH and nanoSiO(2)XDH retained more than 40 % activity and GDH and XDH immobilized on SBA silica maintained around 50 % of their initial activity resulting in about 1.5-1.6 fold increase in biocatalytic productivity compared to the free enzymes.
机译:从生物质液体中直接提升和分离单糖是忽略的区域。在这项工作中,我们通过葡萄糖脱氢酶(GDH,EC 1.1.1.47)和木糖脱氢酶(XDH,EC 1.1.1.175),证明了来自预处理的Birchwood液中的葡萄糖和木糖的酶促产生葡萄糖和木糖。使用两种不同种类的二氧化硅载体材料(二氧化硅纳米粒子)和具有六边形孔(SBA 15二氧化硅)的多孔二氧化硅颗粒进行比较生物催化转换,用于酶固定化。在固定时,两种酶在其热稳定性方面表现出显着的改善碱性pH的鲁棒性,并且在固定基质上的pH10和60℃下表现出超过50%的活性。与45℃的游离酶相比,在纳米烃(2)和SBA二氧化硅上固定的GDH显示4.5和7.25倍分别增加半衰期,同时分别在纳米核苷(2)和SBA上固定的XDH分别显示出半衰期的4.7%和9.5倍。另外,在五次反应循环后,纳米磷(2)GDH和纳米磷(2)XDH保留超过40%的活性和固定在SBA二氧化硅上的GDH和XDH维持在其初始活性的50%约50%,导致生物催化生产率的增加约1.5-1.6倍。相比免费酶。

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